5-arylazo-pyrimidine dyestuffs



United States Patent US. Cl. 260-154 17 Claims ABSTRACT OF THE DISCLOSURE Dispersible dyestulfs which are -arylazo-pyrimidines wherein the carbon atoms in 2-, 4- and 6-positions of the pyrimidine ring are occupied by amino groups at least one of which is substituted by an unsubstituted or nonionogenically substituted phenyl radical and at least one other of which amino groups is substituted by hydroxyalkyl, certain substituted oxyalkyl, or acyloxyalkyl groups; such dyestuffs being distinguished by good affinity especially for polyester fibers, affording dyeings on these fibers which have excellent fastness properties; processes for dyeing polyester fibers with the aforesaid novel dyestufis; and compositions containing polyester fiber material and such novel dyestuffs.

CROSS REFERENCE TO RELATED APPLICATION This application is a continuation-in-part of our pending patent application Ser. No. 567,057 filed on July 22, 1966.

DESCRIPTION OF THE INVENTION The present invention concerns new, slightly or very slightly Water-soluble azo dyestuffs which can be used as dispersible dyes, processes for the production thereof, processes for the dyeing therewith of hydrophobic organic fiber materials, particularly of textile fibers made from linear high molecular esters of aromatic polycarboxylic acids with polyvalent alcohols or from cellulose esters and, as industrial products, the fiber materials dyed with the new dyestuffs.

Difiiculty soluble azo dyestuffs which can be dispersed in water containing no ionogenie groups forming salt in water of formula:

NH-Rs (III) wherein:

A represents the radical of an aromatic homocycle or heterocycle which can contain non-ionogenic substituents including phenyl azo groups, and

of R R and R one R represents an unsubstituted or non-ionogenically substituted phenyl radical and the other Rs each represent hydrogen or an unsubstituted or nonionogenically substituted alkyl, eycloalkyl or phenylalkyl group,

have been described in our patent application Ser. No.

567,057, supra.

It has now been found that azo pyrimidine dyestuffs are obtained which are distinguished by particularly advantageous properties-for example, good fastness to sublimation, colour strength and purity of the polyester dyeings attained therewith, and excellent buildup of the dyes on polyester fibers, when the diazonium compound of an amine of formula:

ANH (I) 3,532,682 Patented Oct. 6, 1970 is coupled with a coupling component of formula NH-Ra to form an azo dyestutf of formula:

NH-Rl NHR: (III) In this process the starting materials are so chosen that the azo dyestuiT obtained is free from ionogenic, saltforming groups, i.e. it contains neither groups which dissociate acid in water such as sulfonic acid, carboxylic acid or phosphoric acid groups, nor onium groups such as ammonium or sulphonium groups.

In the Formulas I, II and III:

A represents an optionally substituted carbocyclic or heterocyclic aryl radical which can also contain arylazo groups,

and of R R and R one R represents an optionally substituted phenyl radical, another R represents a radical of the formula -alk-O-Z wherein -alkrepresents an optionally substituted alkylene radical and Z represents hydrogen, an acyl radical or an optionally substituted hydrocarbon radical, and the third R represents hydrogen or an optionally substituted alkyl, cycloalkyl or phenylalkyl radical.

Preferred azo dyestuffs produced according to the invention are coupling products of Formula III which are produced by using diazonium compounds of amines of Formula I wherein A:

(a) represents a phenyl radical in 0- and/or p-position to the azo group, which phenyl radical contains at least one non-ionogenic, electron attracting substituent, or

(b) it represents an optionally non-ionogenically substituted benzothiazolyl-(Z) radical, or

(c) it represents an optionally non-ionogenically substituted 4-phenylazophenyl radical.

In order to attain the desired sublimation fastness properties and, at the same time, to provide excellent buildup and levelling power on the aforesaid fibers, one R in the azo pyrimidine dyestufis according to the invention must be an optionally non-ionogenically substituted phenyl radical and another R must be the group -alk-O-Z.

As non-ionogenic substituents of the phenyl radical, for example, the substituents conventionally employed in diazo components can be used, particularly lower alkyl or lower alkoxy groups, and halogens.

The chain of the alkylene group -alkcan be straight or branched; in the former case it is preferably the 1,2- ethylene or 1,3-propylene group, in the latter case it is the 1,2-propylene or 1,2-butylene group. Such divalent radicals can be substituted, eg by phenyl, hydroxy or low alkoxy groups such as the methoxy or ethoxy group.

Z, as acyl radical is, particularly, a lower unsubstituted or non-ionogenically substituted alkanoyl group. The alkanoyl radical has, advantageously, two to four carbon atoms. The alkanoyl group can contain, e.g. halogens such as chlorine or bromine, or lower alkoxy groups such as the methoxy or ethoxy group as non-ionogenic substituents.

Z, as hydrocarbon radical represents, e.g. a straight or branched chain alkyl radical having, a preferably, 1 to 4 carbon atoms, a eycloalkyl radical such as the cyclohexyl or methylcyclohexyl radical, an aralkyl radical, particularly a phenylalkyl radical such as the benzyl radical, or a carbocyclic aryl radical such as the phenyl radical. If

these hydrocarbon radicals are substituted, then examples of substituents are halogens such as fluorine, chlorine or bromine, cyano groups, hydroxyl groups or lower alkoxy groups or phenoxy groups.

If one of R R and R represents an alkyl radical, this can contain up to 12 and, in direct chain preferably 1 to 5, carbon atoms and the chain can be normal or branched. If this alkyl radical is substituted, then examples of substituents are the hydroxyl group, alkoxy groups such as unsubstituted alkoxy, alkoxyalkoxy or alkoxyalkoxyalkoxy groups or alkoxycarbonyl groups in each of which the alkoxy unit preferably has 1 to 4 carbon atoms, also acyloxy groups, particularly lower alkanoyloxy groups such as the acetyloxy or propionyloxy group, phenyl, phenoxy, cyano groups or halogens such as fluorine, chlorine or bromine. Examples of cycloalkyl or phenylalkyl groups symbolized by R R or R are the cyclohexyl or methylcyclohexyl groups or the benzyl group, the benzene nucleus of which can contain the non-ionogenic substituents, particularly halogens or lower alkyl or alkoxy groups mentioned hereinbefore in the description of A.

Dyestuffs which, among other things are distinguished by their excellent buildup on polyglycol terephthalate fibers as well as by extraordinary stability in the boiling dyebath and, in addition are very fast to light and sublimation, are derived from coupling components of formula:

wherein of R R and R one R represents an unsubstituted or non-ionogenicall substituted phenyl radical, another R represents a radical of the formula -alkyl-O-Z wherein -alkand Z have the meanings given above, and the third R represents a lower alkyl radical optionally substituted by acyloxy or alkoxy groups.

Of special importance because of their good accessibility are mono-azo dyestuffs according to the invention which fall under the formula:

lower alkylphenylsulfonyl, phenoxysulfonyl, lower alkylphenoxysulfonyl, lower alkoxycarbonyl, hydroxy-lower alkoxycarbonyl, or a substituent of the formula wherein Q represents SO --or-CO R represents hydrogen, lower alkyl, hydroXy-lower alkyl, lower alkoxy-lower alkyl, phenyl, cyclohexyl or benzyl, and

lkRi represents hydrogen, lower alkyl or hydroxy-lower a Y;

(ii) By a second substituent selected from hydrogen, nitro, lower alkyl, lower alkoxy, phenoxy, chlorine and bromine; and

(iii) By a third substituent selected from hydrogen, chlorine and bromine;

(b) A Benzothiazolyl-(Z) radical which is unsubstituted or substituted by chlorine, bromine, nitro, cyano, thiocyano, lower alkyl, lower alkoxy, lower alkylsulfonyl, or a grouping wherein R and R represent lower alkyl;

And disazo dyestuffs falling under Formula III-A wherein A represents 4-phenylazo-phenyl which is unsubstituted or substituted by lower alkyl or lower alkoxy.

In Formula III-A, the remaining symbols have the following meanings for both monoazo and disazo dyestuffs:

R represents phenyl having substituents selected from hydrogen, lower alkyl, lower alkoxy, chlorine, bromine and cyano;

One of R and R represents alkyl of from 2 to 5 carbon atoms substituted by the group O--R which represents hydroxy, lower alkoxy, lower alkoxy-lower alkoxy, hydroxy-lower alkoxy, cyclohexyloxy, phenyl-lower alkoxy, phenoxy, lower alkyl-phenoxy, alkanoyloxy of from 2 to 5 carbon atoms, benzoyloxy, lower alkoxycarbonyloxy, phenylsulfonyloxy, or lower alkyl-phenylsulfonyloxy, and

The other one of R and R represents the same as the first one defined, supra, or hydrogen, alkyl of from 1 to 12 carbon atoms, cyclohexyl or phenyl-lower alkyl.

Preferably, one of the first and second substituents of a phenyl radical A as defined under (a) supra is in oand the other in p-position to the adjoining azo bridge.

More preferred because of especially good fastness properties of their dyeing on polyester fibres are those monoazo dyestuffs falling under Formula III-A having the lastmentioned preferred substitution in the coupling component and, as diazo component the grouping of the formula:

wherein:

one of Z and Z represents nitro,

the other of these Zs represents hydrogen, nitro, cyano, chlorine, bromine or lower alkyl-sulfonyl or lower alkoxy carbonyl, and

2;, represents hydrogen, chlorine or bromine.

Still more preferred in this last-defined subclass of dye stuffs according to the invention due to their particularly good light fastness are those in which A represents:

2-cyano-4-nitro-phenyl, Z-nitro-phenyl, 4-nitro-phenyl, 2,4-dinitrophenyl, 2-chloro-4-nitrophenyl, 2,4-dinitro-6-chloro-phenyl, 2-bromo-4-nitro-phenyl, 2,4-dinitro-6-bromo-phenyl, 2-nitro-4-chloro-phenyl, 2,6-dichloro-4-nitro-phenyl, 2-nitro-4-methylsulfonyl-phenyl, and 2-nitro-4-ethylsulfonyl-phenyl,

and similar groupings, all of which fall under the formula wherein:

Z represents hydrogen, nitro, cyano, chloro or bromo,

Z represents nitro, chloro, bromo or lower alkylsulfonyl,

but preferably nitro, and

2;, has the aforesaid meaning.

Most preferred are those dyestuffs having the meaning of A defined in Formula Ia, and especially in Formula Ib, supra, which in their coupling components have the following substitution:

R represents phenyl having substituents selected from hydrogen, lower alkyl and lower alkoxy, most preferably, however, hydrogen, methyl and methoxy;

one of R and R represents lower alkyl substituted by hydroxyl, lower alkoxy or alkanoyloxy of from 2 to 5 carbon atoms, and

the other R of the pair of R and R represents lower alkyl which is unsubstituted or substituted by lower alkoxy and/ or alkanoyloxy of from 2 to 5 carbon atoms.

The dyestuffs of Formula III-A as defined above are of particularly high aflinity for polyethylene glycol terephthalate fibers, and the dyeings obtained therewith on the latter fibers are of especially satisfactory fastness to light.

In this application and the appended claims the term lower (or low) in connection with an aliphatic radical means a group containing not more than 5 carbon atoms.

As a final aspect of the invention there are provided disazo dyestuffs of the formula:

(R1011; (R14) n NH-Rg (IIIb) wherein:

R represents phenyl having substituents selected from hydrogen, lower alkyl, lower alkoxy, chlorine, bromine and cyano;

one of R and R represents alkyl of from 2 to 5 carbon atoms substituted by the group OR which group represents hydroxy, lower alkoxy, lower alkoxy-lower alkoxy, hydroxy-lower alkoxy, cyclohexyloxy, phenyllower alkoxy, phenoxy, lower alkyl-phenoxy, alkanoyloxy of from 2 to 5 carbon atoms, benzoyloxy, lower alkoxycarbonyloxy, phenyl-sulfonyloxy, or lower alkylphenyl-sulfonyloxy,

and the other one of R and R represents the same as the first one defined, supra, or hydrogen, alkyl of from 1 to 12 carbon atoms, cyclohexyl or phenyl-lower alkyl,

each of R and R 14 represents hydrogen, lower alkyl, or

lower alkoxy,

m represents a number from 1 to 3, and

n represents a number from 1 to 2.

The 2,4,6-triamino-pyrimidine compounds of Formula II usable according to the invention as coupling components, are produced by reacting the three chlorine atoms of 2,4,o-trichloropyrimidine one after the other with ammonia or with primary aliphatic, cycloaliphatic, araliphatic or carbocyclic-aromatic amines as defined. Advantageously less reactive amines are used in the first step and in the second and third step, ammonia and/or easily reacting, more strongly basic amines are used in any order desired. The products resulting from the first step are generally mixtures of isomers of 2amino-4,6-dichloro-pyrimidines and 4-amino-2,6-dichloro-pyrimidines which can be separated, if desired, by recrystallisation or by chromatographic adsorption, e.g. on aluminium oxide. Preferably however, the mixtures of isomers are used as they yield mixtures of azo pyrimidine dyestuffs according to the invention which are distinguished by very good buildup.

The step-wise reaction is performed, e.g. in aqueous organic or organic-aqueous solution or dispersion, optionally in the presence of acid binding agents such as alkali and alkaline earth carbonates or oxides, or tertiary nitrogen bases. Examples of suitable organic solvents are alcohols such as methanol or ethanol, ethylene glycol mon omethyl ether or monoethyl ether, preferably however, adiphatic ketones such as acetone, methylethyl ketone or methylisobutyl ketone, cyclic ethers, e.g. dioxane or tetrahydrofuran, or optionally halogenated or nitratated aromatic hydrocarbons such as toluene, xylenes, chloro-benzene or nitrobenzene.

The first chlorine atom of the 2,4,6-trichloro-pyrimidine is reacted at low temperatures, advantageously at 20-60 C., the second chlorine atom is reacted at moderate temperatures, preferably at 70-100" C., and the third chlorine atoms is reacted at higher temperatures, preferably between and C., optionally in a closed reaction vessel.

If, in the pyrimidine coupling components of Formula II usable according to the invention, of R R and R one R represents a radical of the formula -all -OH and another R represents an alkyl radical which optionally contains one or more hydroxyl groups as non-ionogenic groups, then these hydroxyl groups can be subsequently acylated. For this purpose, the anhydrides of low carboxylic acids such as acetanhydride or propionic acid anhydride, the acyl chlorides and bromides of the aliphatic and aromatic series, e.g. acetyl, propionyl, butyryl or benzoyl chloride or bromide, also chloroformic or bromoformic acid esters, particularly chloroformic or bromoformic acid methyl or ethyl ester, phenyl sulfonic acid chloride or p-methylphenylsulfonic acid chloride are used as acylating agents.

A modification of the process according to the invention for the production of difiiculty water soluble azo dyestuffs of Formula III in which of R R and R at least one R represents an alkyl radical substituted by acyloxy groups, consists in reacting a compound of Formula V wherein of R R and R one R represents an optionally substituted phenyl radical, another R represents a radical of the formula -alk-OH, and the third R represents the same as the second R, an unsubstituted alkyl group, or substituted alkyl group different therefrom or an optionally substituted cycloalkyl or phenylalkyl group, and

A and -alkhave the meanings given above, with an acylating agent, the starting materials being so chosen that the final dyestulf contains no ionogenic groups forming salt in water.

Azo compounds of Formula V are obtained, e.g. by coupling the diazonium compound of an amine of Formula I with the corresponding pyrimidine coupling component, the coupling being performed as described further below.

Acylating agents suitable for the acylation of azo compounds of Formula V usable according to the invention are, e.g. those mentioned above.

The acylation is performed advantageously at a raised temperature in a suitable organic solvent such as glacial acetic acid, chlorobenzene or dioxane, optionally in the presence of an acid binding agent such as sodium acetate, pyridine or magnesium oxide.

The products resulting from the condensation are generally mixtures of isomers of 2-phenylaminc-4,6-dichloropyrimidines and 4-pheny1amino-2,6-dichloro-pyrimidines, which can be separated by fractional crystallization or chromatographic techniques. Often, however, it is preferred to use the crude isomer mixtures as coupling components, because the resulting composite dyes afford superior fastness properties.

The coupling of the diazonium compounds of an amine of Formula I with a coupling component of Formula II is performed by the usual methods, preferably in mineral acid to weakly acid aqueous medium, more especially at a pH of 4-4.5. When coupling in a mineral acid medium, the acid is advantageously gradually buffered, for example, with alkali metal salts of lower fatty acids. It is also possible to simultaneously couple a suitable diazonium compound with a mixture of isomeric coupling components usable according to the invention.

The dyestuffs according to the invention are finely dispersed by milling with surface active dispersing agents. Suitable dispersing agents are, e.g. anionic salts such as alkali metal salts of sec. higher alkylaryl sulfonates, alkali metal salts of condensation products of formaldehyde and naphthalenesulphonic acids, lignin sulfonates, or nonionogenic dispersing agents such as fatty alcohol polyglycol ethers.

Dyestuffs according to the invention possess a very good drawing power and good buildup onto polyglycol terephthalate fibers and, on these fibers, produce strongly coloured greenish yellow, yellow, orange, scarlet and red to bordeaux coloured dyeings which are excellently fast to washing, milling, sublimation, light, rubbing, perspiration, solvents, cross-dyeing, decatising, gas fading and industrial fumes. They form very stable dispersions and, moreover, it is particularly remarkable that when dyeing tightly twisted polyester yarns in the form of cheeses or of polyester slubbing, the azo dyestuffs according to the invention do not tend to form deposits.

In addition, the dyestuffs according to the invention are also suitable for the dyeing of polyolefins, particularly polypropylene fibers.

The dyestuffs which can be obtained according to the invention, particularly the mixtures of isomers, differ from previously known dyestuffs of similar constitution by their very good drawing power and buildup onto polyglycol terephthalate fibers. In addition, dyeings attained with the dyestuffs according to the invention have, in most cases, substantially better fastness to light and sublimation.

Particularly valuable dyestuffs according to the invention which are distinguished by good fastness to sublimation, excellent fastness to light as well as by optimal drawing power, buildup and levelling power, are derived from mixtures of isomers of the formulas wherein:

of Z Z and Z one Z represents the nitro group, a second Z represents hydrogen, the nitro, cyano, methylsulphonyl or ethylsulphonyl group, chlorine or bromine, and the third Z represents hydrogen, chlorine or bromine,

R represents hydrogen, the methyl or methoxy group,

and

of R and R one R represents a low alkyl group substituted by hydroxyl, lower alkoxy or alkanoyloxy of from 2 to 5 carbon atoms, and

the other R represents lower alkyl which is unsubstituted or substituted by alkanoyloxy of from 2 to 5 carbon atoms or lower alkoxy.

The following non-limitative examples illustrate the invention further. The temperatures are given therein in degrees centigrade. Polyglycol terephthalate represents the products known by the trade names Terylene, Vycron, Dacron and Trevira. Parts and percentages are given by weight unless expressly stated otherwise.

Example 1 21.8 g. of l-amino-2,4-dinitro-6-chlorobenzene ar dissolved in 200 g. of concentrated sulphuric acid and, at 2030, the solution is diazotised with an amount of nitrosyl sulphuric acid corresponding to 6.9 g. of sodium nitrite. The diazonium salt solution so obtained is added dropwise, at 0-5", to a solution of a mixture consisting of 23 g. of Z-ethylamino-4-phenylamino-6-,3-hydroxyethylamine-pyrimidine and 4.3 g. of 2-phenylamino-4- ethylamino-6-fl-hydroxyethylamino-pyrimidine in 400 g. of 80% acetic acid and 300 g. of water. On completion of the coupling, the dark red coloured precipitate formed, the composition of which corresponds to the formulae:

is separated by filtration, washed with water and dried in the usual way. g. of the dyestuff mixture so obtained is brought into a finely dispersable form by milling with g. of a lignin sulphonate.

Polyglycol terephthalate fibres can be dyed in pure red shades with this dyestuffs mixture, optionally in the presence of a carrier such as trichlorobenzene. The dyeings obtained have very good fastness to washing, rubbing, light and sublimation.

The mixture used in this example as coupling component consisting of 2-ethylamino4-phenylamino-6-fl-hydroxyethylamino-pyrimidine and 2-phenylamino-4-ethylamin0-6-[3-hydroxyethylaminc-pyrimidine is obtained, e.g. by reacting 2,4,6-trich1oro-pyrimidine with one equivalent of aniline at 50, condensing the mixture of 4-anilino- 2,6-dichloro-pyrimidine and 2-anilino-4,6-dichloro-pyrimidine resulting therefrom with excess ethylamine at to form a mixture consisting of 2-ethylamino-4-phenylamino-6-chloro-pyrimidine and 2-phenylamino-4-ethyl amino-6-chloro-pyrimidine, and reacting this mixture with excess fi-hydroxyethylamine at a temperature of 150.

Dyestuffs having similar properties are obtained when the equivalent amount of each of the diazo components given in column 2 of the following Table I is coupled with any of the mixtures of coupling components given in column 3.

TABLE I Shade on polygly- Ex. col terephthalate No. Diazo component Coupling component fibres 22 .2-meth lamino--(4-methylphenylamlno)-6-B-hydroxyethylamino-pyrirnidine. 2 l'ammo'z'cyano4'nmobenzene {5.3 g. 2-(4mibthyl-phenylamino)-4-methylamindG-B-hydroxyethylamino-pyrnmdinc.}

19 g. 2-methylamlno'4-(2-methoxy-phenylamino)-6-B-hydroxyethylam1no- 3. 1- mino4- itrobenzene yrimidine. a n 5.9 g. 2-(2-methoxy-phenylamino)-4-methylamlno-fi-fl-hydroxyethylammo- Do rimidine. 5K4 g. 2-ethylamino+(2-methoxy-5-methylphenylamino)-6-B-hydroxyethylamlno- 4 2-a ino-G- ethox -benzothiazole rimidine.

m m y g. 2-(2-methoxy-5-methylphenylammo)-4-ethylamlno-fi-B-hydroxyethylamlnopyrimidine. 5 kaminofizobenzene gg f l li l 4 henylamino fi-fi hydroxypropylamino pyrimidine Red.

. .-me yammop 6 ''{5.3 g. 2-pl1enylamino-4-methy1amin0-6 B-hydroxypropylammo-pyrrm drne. 23 g. 2-isopropylamino-4-phenylamino-6-fi-hydroxyethylamino-pyrimldine. 7 "l5.7 g.2-phenylaminoi-isopropylamino-fi-fl-hydroxyethylarmno-pyrnnrdme. I {25.4 g. 2-- -meth0xypropylaminoA-phenylamino-G-B-hydroxyethylamlno-pyrlmidine. 8 6.3 g. 2-phenylamino-4- -methoxypropylamino-G-B-hydroxyethylaminopyrnnidine.

Example 9 is separated by filtration, washed with a large quantity of water and dried in vacuo at 60-70. After millin with A fine Suspenslon of of l'ammobenzeneA-cap do the sodium salt of a condensation product of naphtli alenebOXYIiC acid ethyl ester in 400 of water 30 of 36% 2-sulphonic acid and formaldehyde, the dyestuffs so obhydrochloric acid and g. of cetyl polyglycol ether i tained dyes polyglycol terephthalate fibres from an aquediazotised in the usual way at 05 by the addition of 6.9 0115 dispersion, p p y in the P 6561106 Of a Carrier Such g. of sodium nitrite. The diazonium salt solution obtained 25 as o'phenylphenol m pure yellow shades" The dyebath o is substantially exhausted. The dyeings have very good 15 Clanfied at added dropwlse to a solullon fastness to washing, rubbing, light and sublimation. Close- Of a miXtllfe 0f of 2-ethylamlno-4-Phe11Y1am1I10- ly woven fabric and tightly twisted yarns are also well 6-fl-hydroxyethylamino-pyramidine and 5.5 g. of Z-phenpenetrated and evenly dyed. ylamino 4 ethy1amin0 6 fi hydroxyethylamino pyrimi Dyestuffs havlng srmrlar properties are obtained when dine in 800 g of acetic acid The PH of the mixture the equ1valent amount of each of the diazo components given in column 2 of the following Table II is coupled 1s then ralsed to 44.5 by the addltlon of sodium acetate. with the mixture of coupling components used in the On completion of the coupling, the preclpitated yellow above example.

TABLE II Shade on polygly- Ex. col terephthalate No. Diazo component Coupling component fibres 23 g. 2-eth ylamin0-4-phenylamino-G-B-hydroxyethylamino-pyrimidine lammo'gfldlcmm obemene "{43 g. 2-phenylamino-4-ethylamino-fi-fl-hydroxyethylamino-pyrimidine. l-amino-2-nitrobenzene Same as above Yellowish orange Lamino-2-nitro-4-methylbenzene. d0 Orange. 1-amino-2nitro-4-mcthoxybenzene -do- Scarlet. l-amino-Z-nitrot ehlorobenzene .d0.. Reddish orange. 15 l-aminoQ-nitro-tmethylsulphonyldo Scarlet.

benzene. 16 1-amino-2-chloro-4-nitrobenzene d0 Do.

l-aminoQ-rnethoxyA-nitrobenzene.. do Red. Lamina-2,6-dich1oro-4-nitrobenzenedo.. Scarlet. l-amino-2,5-dichloro-4nitrobenzene.. do.- Yellow-brown. l-amino-Z-bromoA-nitrobenzene-.. .d0- Scarlet. 1-amino-Z-cyano knitrobenzene d0.. D Lamino4-methylsulphonyl-benzene ..do- Yellow. l-aminobenzene-rsulphom'e acid-N- do D0.

phenylamide. 24 l-aminobenzene-i-sulphonic aciddo Do.

dimethylarnide. 25 l-aminobenzene-4-carboxylic aciddo Do.

propylamide. 26... i-amino kacetylbenzene do Reddish yellow 2-amino-6-methoxy-benzothiazole d0.. car-let. Z-amlno-S-cyano-benzothiazole .do Do. 2-amino-G-thiocyanobenzothiazole d0 Do. 2-an1ino6-methylsulphonyldo Scarlet.

benzothiazole. 31 4-amino-2-methylquinoline .d0 Do. 32-.. Gamino-indazole.-. .do Yellow. 3"... 3-amino-indazole ..(lo Do.

coloured precipitate, the composrtron of which corre- Example 34 s ends to the formulae:

p 5 13.8 g. of 1-am1no-4-n1trobenzene are finely slurried NH- In 400 g. of water and 30 g. of 36% hydrochloric acid with the addition of 5 g. of cetyl polyglycol ether and N then diazotised in the usual way at 0-5 by the addition C2115OOC N=N NH C2H2+ of 6.9 g. of sodium nitrite in g. of water.

N The diazonium salt solution obtained is clarified and,

Eg at 510, is added dropwise to a solution of 24.2 g. of 2- 1 N 2 6 ethyl-amino-4-(2'-methoxyphenylamino) 6 ,B-hydroxyczmo O ethylamino pyrimide and 6.1 g. of 2-(2'-methoXy-phenylamino)-4-ethylamino 6 {3 hydroxyethylamino-pyrimidine in 500 g. of acetic acid and 300 g. of water.

The coupling mixture formed is then buffered by the addition of sodium acetate. On completion of the coupling, the scarlet coloured precipitate formed, the composition of Which corresponds to the formulae:

NHC2U5 (J U 113 I N l f W-Q N is separated by filtration, Washed with water and then NIL-01120112011 dried in the usual way. g. of the dyestulf mixture so obtained are brought into a finely dispersable form by milling with 30 g. of a lignin sulphonate. Polyglycol terephthalate fibres can be dyed in pure scarlet shades with this dyestutf mixture, optionally in the presence of a carrier such as trichlorobenzene. The dyeings have very good fastness to rubbing, light and sublimation.

The mixture of 2 ethylamino 4 (2' methoxyphenylamino) 6 ,8 hydroxyethylamino pyrimidine and 2 (2' methoxyphenylamino) 4 ethylamino 6-6- hydroxyethylamino pyrimidine used in this example as coupling component is obtained, eg by reacting 2,4,6- trichloro pyrimidine with one equivalent of l-amino-Z- methoxybenzene at 40-50, condensing the mixture of 4- (2-methoxyphenylamino) 2,6 dichloro-pyrimidine and 2-(2-methoxyphenylamino) 4,6 dichloro-pyrimidine resulting therefrom with excess ethylamine at 8090 to form a mixture of 2 ethylamino 4-(2-methoxyphenylamino) 6 chloro pyrimidine and 2 (2-methoxyphenylamino) 4 ethylamino 6 chloro pyrimidine and reacting this mixture with excess B-hydroxyethylamine at a temperature of 140-150.

Dyestuffs having similar good properties are obtained when the equivalent amount of each of the diazo components given in column 2 of the following Table III is coupled with one of the coupling components or mixture of coupling components given in column 3.

salt solution obtained is added dropwise, at 010, to a solution of a mixture of 24.2 g. of 2 ethylamino 4-(4'- methoxy phenylamino) 6 ,8 hydroxyethylamino-pyrimidine and 6.1 g. of 2 (4 methoxyphenylamino)-2- ethylamino 6 fl hydroxyethylamino pyrimidine in 500 g. of 80% acetic acid and 300 g. of water. The coupling mixture formed is then buffered by the addition of sodium acetate. On completion of the coupling, the dark red coloured precipitate formed, the composition of which corresponds to the formulae:

is separated by filtration, washed with a large quantity of water and dried under reduced pressure at 70-80". 10 g. of the dyestufi mixture so obtained are brought into a finely dispersable form by milling with 20 g. of a lignin sulphonate. Polyglycol terephthalate fibres can be dye in pure red shades with this dyestuff mixture, optionally in the presence of a carrier such as o-phenylphenol. The dyeings have very good fastness to washing, rubbing, perspiration and sublimation.

The mixture of 2-ethylamino 4 (4-methoxyphenylamino)-6-B-hydroxyethylamino pyrimidine and 2 (4- methoxyphenylamino) 4 ethylamino 6 {3 hydroxyethylamino-pyrimidine used in this example as coupling component is obtained, e.g. by reacting 2,4,6-trichloropyrimidine with one equivalent of l-amino-4-methoxybenzene at 40-50, condensing the mixture of 4-(4- methoxy phenylamino) 2,6 dichloro pyrimidine and 2 (4' methoxy phenylamino) 4,6 dichloro-pyrimidine resulting therefrom with excess ethylamine at 8090 to form a mixture of 2-ethylamino-4-(4-methoxy-phenylamino) 6 chloro-pyrimidine and 4 ethylamino 2-(4- methoxy phenylamino) 6 chloro-pyrimidine, and re- TABLE III Shade on polygly- Ex. col terephthalate No. Diazo component Coupllng component fibres 19.5 g. 2-amino-4-phenylamino-fi fi-hydroxycthylamino-pyrimidine. 1 2 cl'florobemene '{4.9 g. 2-phenylamlnoA-amino-6-B-hydroxyethylamino-pyrimidine. 36 l-amrnoA-nrtrobenzene Same as above. Orange. 37 Lamkiolienene4-carboxylic acid 2463 g. Z-propylamino-4-(4-hydroxyphenylamino)-6-fl-hydroxyethylamino-pyrimime y es er. me.

61 2(4-l1ydroxyphenylamino)-4-propylamino-6;3-hydroxyethylamino-pyrimi- Reddlsh yellow me. .0 g. 2 butylamino-4- (4 -chlo1opl1cnylamin o) -6-fl-hydroxyethylamino-pyrimidine. 38 2:2(4-cl1lgr0pl11enylan;i1in)-4-butylamino-6-B-hydroxyt;thylamino-pyiimidine. Yellow g. -cyc o exy amiuo- -pl1eny amino-fi-B-hydroxyethy amino-py1imidine. 1 ammo 2 037M104 nltlobenzene "i267 gprenylpmino-ficyglohtixylamino-6-B-hydr0xyfithylamino-pyrimidine. scarlet g. enzy aminop eny amino6-fi-hydroxy-et y aminopyrimidine. 1 ammo 4 Intro benzene {5] g. 2-phenylamino-4-benzylamino-G-B-hydroxyethylaminopyrimidine. Reddlsh Orange {22.5 g. 2-ethylamino-4-(2methylphenylamino)-6-B-hydroxy-propylamino-pyrimidine. D 0

"""""""""""""""" 7.5 g. 2-(2-methylphenylamino) 4-ethylamino-6-B-hydroxy-propylamino-pyrimidine.

42 do {22.3 g. 2-ethylamino-kphenylamino-G-fi-hydloxybutylaminopyrimidine. D

"""""""""""""""""""""" 3 8 2- Dl r nylamlnozi-tfihylzimino-fi-iS-hlydoxybutylaminopyrimidine.

g. -e yamino- -p eny amino-fi-B- y roxy-'y-methoxy-propylamino-pyrimidine. 1 amlmo chloro! lfi2 g. 2-phenylamino-4-ethylamino-G-B-hydroxy-v-methoxy-propylamino-pyrimidine. Scarlet 44 l-amrnobenzene-4-carboxyl1c acid {28.0 g. 2-ethylamino-4-phenylamino-G-B-hydroxy-fi-phenylethylamino-pyrimidine. 11

methylamlne 6.8g. Z-phenylamino-4-ethylamino6-B-hydroxy-B-phenylethylamino-pyrimidine. J 9 45..." 1-arn1no-2,4-dinltl'o-fi-bromobenzene 2-ethylam1no4-phenylamino-G-B-hydroxy-ethylaminopyrimidine. Red. 46 "do if-5hycg'gxytelthylazrgiipo l-phenfilamiilo-6-ethylamino-pyrimidine. d lRed.

g. -c oroe y amino-4p ieny amino6B-l1ydroxyethy amino-pyrimi ine. 1 r methylbenzene' "{62 g. 2-phenylam1no-4-B-chloroethylarnino-fi-B-hydroxyethylarnino-pyrimidine. l 47a 1-am1n0-2A-d1mtro-6-chlor0benzene 4-ethylarnino-2-phenylamino-6(B-hydroxy-ethylamino)pyrimidine. Re

471) l-amino-benzene-tcarboxylic acid phenylamide.

4,6-bis-( -methoxy propylamino) -2-phenylaminopyrimidine.

d. Reddish-yellow.

Example 48 A fine suspension of 17.3 g. of 1 amino 2 chloro-4- nitrobenzene in 300 g. of water, 30 g. of 36% hydrochloric acid and 5 g. of cetyl polyglycol ether is diazotised at 05 by the dropwise addition of a solution of 6.9 g.

acting this mixture with excess ,B-hydroxyethylamine at a temperature of 140-150.

If in the above example, the mixture of 2-ethylamino- 4-(4-methoxyphenylamix1o) 6 B hydroxyethylaminopyrimidine and 2 (4' methoxyphenylamino) 4 ethylof sodium nitrite in 50 g. of water. The clear diazonium amino 6 ,8 hydroxyethylamino-pyrimidine used as coupling component is replaced by the same amount of a mixture of 2 B hydroxyethylamino 4 (4' methoxyphenylamino) 6 ethylamino-pyrimidine and 2 (4'- methoxyphenylamino) 4 fl hydroxy ethylamino 6- ethylamino-pyrimidine, then a dyestulf mixture is obtained which produces pure red dyeings having similarly good properties on polyester fibers.

Example 49 18 g. of 2-amino-6 methoxy-benzothiazole in 100 g. of concentrated sulphuric acid are diazotised for 3 hours at 5 with nitrosyl sulphuric acid, corresponding to 6.9 g. of sodium nitrite. The diazonium salt solution so obtained is added dropwise, at -5", to a solution of 23 g. of 2-isopropylamino 4 phenylamino 6 ,8 hydroxyethylamino-pyrimidine and 5.7 g. of 2-phenylamino-4-isopropylamino 6 B hydroxyethylamino-pyrimidine in 400 g. of 80% acetic acid and 250 g. of Water. On completion of the coupling, 500 g. of Water are added to the reaction mixture obtained. The precipitated scarlet dyestuff precipitate is then separated by filtration, washed with water and then dried in the usual way. 10 g. of the dyestufi' mixture so obtained, the composition of which corresponds to the formulae:

NHOH(CH3):

CHaO- are brought into a finely dispersable form by milling with 20 g. of a lignin sulphonate. Polyglycol terephthalate fibres can be dyed in pure scarlet shades with this dyestuff mixture, optionally in the presence of a carrier such as trichlorobenzene. The dyeings have very good fastness to washing, perspiration, decatising, light and sublimation.

The mixture of 2-isopropylamino-4-phenylamino-6-5- hydroxyethylamino-pyrimidine and 2 phenylamino 4- isopropylamino 6 3 hydroxyethylamino-pyrimidine used in this example as coupling component is obtained, e.g. by reacting 2,4,6-trichloro-pyrimidine with one equivalent of aniline, condensing the mixture of 4-phenylamino-2,6-dichloro-pyrimidine and 2-phenylamino-4,6-dichloro-pyrimidine resulting therefrom With excess isopropylamine at 80-90 to form a mixture of 2-isopropylamino-4-phenylamino-6-chloro-pyrimidine and 2-phenylamino-4-isopropylamino-6-chloro-pyrimidine, and reacting this mixture with excess ,B-hydroxyethylamine at a temperature of 140160.

Example 50 A fine suspension of 19.7 g. of 4-amino-azobenzene in 500 g. of Water, 75 g. of 36% hydrochloric acid and g. of oleyl polyglycol ether is diazotised in the usual Way at l520 by the addition of 6.9 g. of sodium nitrite. The diazonium salt solution formed is added dropwise, at 10- to a solution of a mixture of 21.8 g. of Z-methylamino 4 phenylamino 6 'y hydroxypropylamino pyrimidine and 5.5 g. of 2-phenylamino-4-methylamino-6- 'y-hydroxypropylamino-pyrimidine in 500 g. of 80% acetic acid and 400 g. of water. The pH of the reaction mixture obtained is then raised to 44.5 by the addition of sodium acetate. On completion of the coupling, the red coloured dyestuif precipitate formed, the composition of which NHOHzOHzCHzOH is separated by filtration, washed with water and dried in the usual Way. 5 g. of the dyestufi mixture obtained in this Way are brought into a finely dispersable form by milling with 12 g. of sodium salt of a condensation product of naphthalene-Z-sulphonic acid and formaldehyde. Polyglycol terephthalate fibres dyed in pure scarlet shades are obtained with this dyestuff mixture by dyeing from aqueous dispersion, optionally in the presence of a carrier such as o-phenylphenol. The dyeings have very good fastness to Washing, rubbing and perspiration.

The mixture of 2 rnethylamino 4-phenylamino-6-yhydroxypropylamino pyrimidine and 2 phenylamino-4- methylamino 6 'y hydroxypropylamino pyrimidine used in this example as coupling component is obtained, egg. by reacting a mixture of 4-phenylamino-2,6-dichloropyrimidine and 2 phenylamino 4,6 dichloro pyrimidine with excess methylamine at -90 and condensation of the mixture of 2-methylamino-4-phenylamino-6- chloro pyrimidine and 2 phenylamino 4 methylamino 6 chloro pyrimidine resulting therefrom With excess *y-hydroxypropylamine at a temperature of If the mixture of Z-methylamino-4-phenylamino-6-yhydroxypropylamino-pyrimidine and 2-phenylamino 4- methylamino-6-v-hydroxypropylamino pyrimidine used in the above example as coupling component is replaced by the same amount of a mixture of 2-B-hydroxypropylamino 4 phenylamino 6 rnethylamino pyrimidine and 2 phenylamino 4 p hydroxypropylamino 6- methylamino-pyrimidine, then a dyestuff mixture is ob tained which produces pure scarlet dyeings having similarly good properties on polyglycol terephthalate fibres.

Example 51 21.8 g. of 1-amino-2,4-dinitro-6-chlorobenzene are dissolved in 200 g. of concentrated sulphuric acid and, at 2030, the solution is diazotised in the usual way with nitrosyl sulphuric acid. The diazonium salt solution is added dropwise, at 0.5 to a solution of 37.3 g. of 4-phenylamino-2,6-bis-[3-acetoxy-ethylamino-pyrimidine in 400 g. of 80% acetic acid, 250 g. of Water and 200 g. of methyl alcohol. On completion of the coupling, the precipitated dark red coloured precipitate, the composition of which corresponds to the formula:

N02 NH-CHzOHzOCOOHa is filtered ofi, washed with Water and then dried in the usual Way. 10 g. of the dyestuff so obtained are brought into a finely dispersable form by milling with 20 g. of a lignin sulphonate.

Polyglycol terephthalate fibres can be dyed in pure red shades With this dyestuff preparation, optionally in the presence of a carrier such as o-phenyl-phenol. The dyeings obtained have very good fastness to Washing, rubbing, light and sublimation.

The 4-phenylamino-2,6-bis-p-acetoxy-ethylamino-pyrimidine used in this example as coupling component is obtained, egg. by reacting 4-phenylamino-2,6-d-ichloro-pytion product of naphthalene-Z-sulphonic acid and formalrimidine with excess ethanolarnine at a temperature of dehyde. Polyglycol terephthalate fibres can be dyed in 130-170" and then acetylating the resultant 4-phenylamipure scarlet shades with this preparation, optionally in no-2,6-bis-fl-hydroxy-ethylamino-pyrimidine with acetahythe presence of a carrier such as trichlorobenzene. The dride, preferably dissolved in chlorobenzene, at a temdyebath is substantially exhausted. The dyeings have very perature of 7590. 5 good fastness to rubbing, light and sublimation. The rniX- Dyestufis having similar properties are obtained when ture consisting of 2-methylamino-4-phenylamino-6- y-meththe equivalent amount of each of the diazo components oxy-propylamino-pyrimidine and 2-phenylamino-4-methgiven in column 2 of the following Table IV is coupled ylamino-6-'y-methoxy-propylamino-pyrimidine used in this example as coupling component is obtained, e". by reactwith any of the, or a mixture of the, coupling compo- 10 ing a mixture of 4-phenylarnino-2,6-dichloro-pyrimidine nents given in column 3.

TABLE IV Shade on polygly- Ex. col terephthalate N0. Diazo component Coupling component fibres 52 1-amino-4-nitrobenzene 2-amino'4-(2-methylphenylamino)-6-(fl-propoxy-cthylamino)-pyrimidine Yellowish orange. 53... l-amino-2-cyano-4-nitrobenzcne 2-ethylaminoi-phenylamino-6(-y-acetoxy-propylamino)-pyrimidine Scarlet. 54 l-amino-2-ehloro-4-nitrobenzone. 2-methylamino-4-(4methoxyphenylamino)-6-(B-acet0xy-propylamino)-pyrimidine Do. 55..-. 1-amino-2-nitrobenzene 2-methylamino-4-phenyla1nino-6-(fl-butoxy-ethylamino)-pyrimidi11e Yellowish orange.

Ye low.

56...; l-aminot-methyl-sulphonylbenzene Z-(B-aoctoxyethylamino)-4-phcny1arnino'6-(fi-hydroxyethylamino)-pyrimidine 32 g. 4-phenylamino2,6-(bis-[i-acctoxy-ethylamino)-pyrimidiue l'ammo'zii'dmltlobenzene 5.3 g. 2-pheny1a1nino-4,6 (bis-18-acetoxy-ethylamino)-pyrimidine 58 1-amino-2,4-dinitro-G-chlorobcnzene. Same as above 59 l-arnino-2,4dinitro-6-bromobenzene "do 61. 1-amino-4nitrobenzene 2-ethylamino+phenylamino B-hydroxy-ethox ropy1amin0-py1'imidine 62 .do 2-ethylaminoA-phenylamino-o ii-cyclohexyloxy-ethylamino-pyrimidine Do. 63 "do 2-cthylamino-4-phenylamino-6-B-4-methy1phenoxy-ethylamino-pwimidine Do. 64... 1-arnino-4-nitrobcnzene 2-ethylarnino-4-(2-brornophenylamino)43-6-11ydroxyethylamino-pyrimidine 65 do 2-cthylan1ino-4-(4-cyanophenylamino)-6-;3-hydroxyethylamino-pyrimidine 4.3 g. Z-ethylaminc-4-phonylarnino-G-B-hydroxyethylamino-pyrimidine '"{23 g. 2-phenylamino-4-cthylamino-G-B-hydroxyethylamino-pyrimidine.

67. 1-amiuo-4-nitrobenzcne Same as above 68"... l-nmiuo-2-chloro-4-1iitro-bcuzone do 69... Q-amino-G-methoxy-beuzothiazolo.. do 70 d 6.1 g. 2-ethylaminoi-(2-metl1oxyphenylamino)-6-B-hyd1'oxyethylami py I DO 24.2 g. 2-(2-rneth0xyphenyla1nino) 4-etliylamino-fi-fi-hydroxyethylamino-pyrimidine.j 71..." l-ainin04-nitr0benzcne "do o. 72 d {5.3 g. 4phenylamino-2,6-(bis-6-acetoxyethylamino)pyrimidine. N} Do 32 g. 2-phenylarnino-4,6-(bis-B-acetoxy-cthylamino)-pyrimidine Example 73 and 2-phenylamino-4,6-dichloro-pyr1m1d1ne with excess 18 g. of 2-arnino-6-methoxy-benzothiazole in 100 g. of miathylamine at 8.0 90 to form f mi of z'methyla concentrated sulphuric acid are diazotised for 3 hours at i and i f with nitrosyl sulphuric acid corresponding to 6.9 m no-4-methylam1no-6-chloro-pyr1m1d1ne and reacting this of sodium nitrite. The diazonium salt solution so obmlxture Wlth excess Tmethoxypmpylamme at p tained is added dropwise, at 0-5", to a solution of a IlllX- ture of 140450; ture consisting of 24.4 g. of Z-methylamino-4-phenylami- Dyestuffs havlng slmllar good Propertles a Obtalned when the equivalent amount of each of the diazo compono-6-'y-methoxy-propylamino-pyrimidine and 4.3 g. of 2- phenylamino-4-methylamino-6-v-methoxy propylaminonents given in column 2 of the following Table V are pyrimidine in 500 g. of 80% sulphuric acid and 300 g. of coupled with one of the, or with a mixture of the, coupling water. On completion of the coupling, the precipitated components givenincolumn 3.

TABLE V Shade on poly- Ex. glycol terephthal- No. Diazo component Coupling component ate fibres 74 l-arnino-Z-cyano--nitrobenzene 2-cyclohegylamino-4-(4-methylphenylamino)-6-('y-methoxyethoxypropylamino)- Scarlet.

pynmi ine. 75 l-aminoA-nitrobenzene 2 propylamino-4-phenylamino-ti-( 6-phenoiq -ethylamino)-pyru111d1ne. Orange. 76 do 2-1(111iethylamino-4-(2-methoxypheuylammo)-6-(7benzyloxypropylammo)-pyr1mi- Do.

no. 77"-.. 1-amino-2,4-dinitrobenzene g-('y-mgthcity-E yla iniifio)-4-Phenylainzino-63thylaminoipyrimidine a Red.

-6.7 g. -propy amino- -p eny ammoy-me oxy-propy amino -pyr1m1 lne "{4.8 g. Z-phenylamino-4-propylamino-6- (y-methoxy-p ropylamino) -pyrimidine red coloured precipitate, the composition of which corre- Example 79 sponds to the formulas: 45.2 g. of the dyestuff mixture produced according to example 34, the composition of which corresponds to the N HQ formulae: i CHaO is filtered off, washed with water and then dried in the NH-CH2CH2OH usual way. 10 g. of the dyestutf mixture so obtained are are slurried in 250 g. of glacial acetic acid. 20 g. of the finely milled with 25 g. of the sodium salt of a condensaacetanhydride are then added to the fine suspension and 17 the whole is heated for 2 hours at 70-85 40 g. of methyl alcohol are then added to remove excess acteanhydride and the reaction mixture is kept for another 2 hours at 5060. The acetylated dyestufi mixture, the composition of which corresponds to the formulae 18 Example 104d 42.3 g. of the mixture of dyestuffs produced according to Example 10421, the composition of which corresponds to the formulae:

0112? NH N OzN-N=N NHC2H O2N- N=N --NHC2H5 NH CH2OH2OH N NH-C2H5 NHOH2OH2OCOCH3 N N o N- 2 Q N NH Q NH CH2CH2OCOCH3 are slurried in 400 g. of dioxane. 10 g. of magnesium is then completely precipitated by the addition of 250 g. Oxlde P 13 5- of benzoyl chlonde are addgd to the of water, filtered off, washed with water and dried in the Suspenslon Whlch h heated for hours 90-95 usual way at 6 7() under d d pressure 10 g. f the The hot dyestutf solution 1s then clarified, the dioxane 1s dyestufi mixture so obtained are brought into a finely disremoved Wlth Steam and, after e g, the Wale? 15 persable form by milling with 20 g. of a lignin sulphonate. Cahted- The behzoylated dystllfi then taken P 111 2500 Polyglycol terephthalate fibres can be dyed in pure scarof hot methyl el whereupon the IhlXture of y let shades with this preparation, optionally in the presence Stufi5 the cempesltloh of which corresponds t0 the formuof a carrier such as o-phenylphenol. The dyeings obtained lee: have very good fastness to washing, rubbing, light and sublimation. NH

Dyestuffs having similar properties as the dyestuff obtained by the procedure described in Example 9, are obtained by repeating the latter example, but using as diazo N component an equivalent amount of a diazonium salt ob- NH CHZCHZOCO* tained by diazotizing in a conventional manner each of NH-CHzH5 the amines given 1n the second column of the following N Table VI, and coupling the said diazonium salt with one O2N- NN NH of the coupling components listed in the th1rd column of Table VI. The resulting dyestuffs dye polyethyleneglycol terephthalate fibers in the shades given in the last column NH- CH2CH2OCO of that table.

TABLE VI Shade on polyglycol terephthalate Diazo component Coupling component fibers 1-amino-3-nitro-4'fluoro-benzene. 2-et ylamino-4-phenylamino-6B-hydroxyethylaminopyrimidine Yellowish orange. l-aminct-trifluor0methylbenzene. Yellow. l-arniuoA-benzoylbenzene. D0. l-aminoi-pheuyl sulfonyl-b ze D0. l-amiuoA-(4-methylphenyl)- D0.

sulionylbcnzene. l-amiuo-Z-nitro-benzene-i-sultonic Scarlet.

aeid-phcnylcster. l-aminoQ-nitro-bcnzene-4sulf0nic D0.

acid4-methylphenyl-ester. l-amino-4-6-hydroxyethoxy Yellow.

carbonyl-benzene. 1amino-4-sulfamoylb enz ene -do Do. l-amino-2-nitrobcnzenc-4-suli0nic do Scarlet.

acid-N-methyl-N-fl-hydroxyethylamide. l-amino-Z-nitro-benzene-4-sull0nic do Do.

acid-- -methoxy propyl-amide. 9l. l-amino -nitro-beuzenc-l-sulfonic do .4 Do.

acid-cyclodiexylamide. 92 l-amino-2-nitro-benzcne-4-sulfouic do D0.

aci dNbcnzyl-N 3-11ydroxycthylamide. 93.. l-amiuo-Z-nitrobenzcne-4-carboxy1ic ..do Do.

acidfl-hydroxyethylamide. 94"-.. l-amino-benzcne-4-carboxylic aciddo Yellow.

'y-mcthoxypropylamide. 95-.. l-amino-benzenei-carboxylic acid- -.do Do.

N-phenyl-N-methyl amide. 96.. l-amino-benzcne-i-carboxylic acid- ..do Do.

cyelO-hexylamide. 97... l-amino-2-nitrobenzenel-carboxylic do Scarlet;

acid-N-benzyl-N-Bhydroxyethylamide. 98 1-amino-2-nitro-4-phenoxy-benzene d0 Red. 90 2-amino-benz0thiazole ..d0.. Orange. 100.... Z-amindfichlorobenzo-thiazole do.. Scarlet. 101.-.. Z-arnino-G-bromobenzo-thiazole d0.. Do. 102.... 2-amlno-6-nitrobcnzothiazole 2-ethylamino-4-phenylamino-6-BJ1ydroxyethylaminopyrimidine. Do. 103 Z-amino-fianethylbenzo-thiazole .do Orange 104.... 2-amino4 beuzothiazole-fi-sulfonic Scarlet.

acid-dimethylamide. I) 2 th I 4 l I 65h d U 1 I d g. -e y ammo- -p ieny aminoy roxye 1y amrno-pyrnm me 104m" lmnmo4'mtrobenzene "{43 g. 2-pl1enylamino-4-ethylamino-6-Bhydroxyethylamino-pyrimidine 1041).. l-ami0n-2-metl1yl-4nitrobenzene .do Do. 1040... 1-amino-2-nitro-benzcne do Yellowishorange.

19 precipitates in crystalline form during cooling. This precipitate is then filtered off and dried in the usual way. g. of the mixture of dyestuffs so obtained is brought into a finely dispersible form by milling with g. of a lignin sulphonate.

Polyglycol terephthalate fibres can be dyed in pure orange shades with this preparation, optionally in the presence of a carrier such as o-phenylphenol. The dyeings obtained have very good fastness to rubbing, light and sublimation.

Dyestuffs having similarly good properties are obtained if, in the above Example 104d, instead of 13 g. of benzoyl chloride, the equivalent amount of either propionic acid chloride, butyric acid chloride, chloroformic acid rnethyl or ethyl ester, benzene sulphonic acid chloride or p-toluene sulphonic acid chloride is used.

Example 105 Polyglycol terephthalate fabric (such as Dacron) is impregnated in a padding mangle at with a liquor of 4 the following composition:

The fabric, squeezed out to a content of about 100% impregnation liquor, is dried at 100 and then fixed for 30 seconds at a temperature of 210. The dyed goods are rinsed with water, soaped and dried. Under these conditions, a scarlet dyeing as obtained which is fast to washing, rubbing, light and sublimation.

The dyestuffs described in the other examples produce dyeings of equal quality by this process.

Example 106 In an apparatus for dyeing under pressure, 2 g. of the dyestuff obtained according to Example 58 are finely suspended in 2000 g. of water which contains 4 g. of oleyl polyglycol ether. The pH of the dye bath is adjusted to 55.5 with acetic acid.

100 g. of polyglycol terephthalate fabric are then introduced at the bath is heated to 140 within 30 minutes and dyeing is performed for 50 minutes at this temperature. The dyeing is then rinsed with water, soaped and dried. On keeping these conditions, a pure red dyeing is obtained which is fast to washing, perspiration, light and sublimation.

The dyestuffs described in the other examples produce dyeings of equal quality by this process.

Example 107 2 g. of the dyestuff obtained according to Example 1 are dispersed in 4000 g. of water. 12 g. of sodium-o-phenylphenolate are added to this dispersion as carrier and also 12 g. of diarnmonium phosphate are added. 100 g. of polyglycol terephthalate yarn are dyed for 1% hours at 95 98. The dyeing is rinsed and after-treated with dilute sodium hydroxide solution and a dispersing agent.

In this way a pure red dyeing which is fast to washing, light and sublimation is obtained.

If in the above example, the 100 g. of polyglycol terephthalate yarn are replaced by 100 g. of cellulose triacetate fabric, dyeing is performed under the conditions given and then the dyeing is rinsed with water, then a red dyeing having a very good fastness to washing and sublimation is obtained.

The individual isomers of pyrimidine coupling components are produced by a procedure described in the following examples:

Example 108 (a) 93 g. of aniline are suspended in a mixture of 400 g. of water and 200 ml. of acetone, and 8 g. of anhydrous sodium acetate are added dropwise thereto; 183.4 g. of 2,4,6-trichloro-pyrimidine dissolved in 200 ml. of acetone are then added dropwise and, while maintaining the reaction mixture at a temperature of 50-55", 40 g. of sodium hydroxide dissolved in 160 g. of water are added at such a rate that the pH of the reaction mixture remains between 5 and 6 throughout the addition of the trichloropyrimidine. Stirring is then continued at the same temperature range for 4 hours, whereupon the acetonic phase formed is separated from the supernatant aqueous phase, and the acetonic phase is then evaporated to dryness.

The residue consists of a mixture of 85% by weight of 4-pheny1amino-2,6-dichloro-pyrimidine and 15% by weight of 2-phenylamino-4,6-dichloro-pyrimidine; it is then dissolved in 500 ml. of -warm benzene, and, upon cooling, 56.4 g. of the 4-phenylamino isomer crystallize (M.P.135-136).

The mother liquor is then evaporated to dryness and redissolved in 280 ml. of benzene having a temperature of 80. Upon cooling, another 101 g. of 4-phenylamino-2,6- dichloropyrimidine (M.P. 135-136) crystallize. The final mother liquor separated from the crystals, can then be used for isolating the Z-phenylamino isomer therefrom. The second batch of crystals of the 4-phenylamino isomer obtained is still sufiiciently pure to be used together with the first batch in the production of azo dyestuff coupling components therefrom on an industrial scale.

(b) 48 g. of 4-phenylamino-2,6-dichloro-pyrimidine obtained from step (a) are dissolved in 100 g. of dioxan, and 160 g. of water are added to the solution; to the resulting suspension there are added 30 g. of ethylamine in 30 g. of water, the reaction mixture is then heated to 90 during 6 hours with stirring, and stirring is continued while the mixture cools down to room temperature. Technically pure 4-phenylamino-2-ethylamino 6 chloro pyrimidine having a melting point of about precipitates and is separated by filtration and dried.

(c) 50 g. of the latter product are mixed with 30 g. of undiluted Z-amino-ethanol, and the mixture is heated with stirring at 140l50 for 2 hours. 4-phenylamino-2-ethylamino 6 (ti-hydroxyethylamino)-pyrimidine of syrupy consistency is obtained which can be used directly as coupling component in the production of dyestuffs according to the invention.

Example 109 (a) The second mother liquor obtained as described under (a) in Example 108 is evaporated to dryness and a residue of 43.1 g. of crude 2-phenylamino-4,6-dichloropyrimidine (M.P. 90-91") is obtained.

5 g. of this crude product are dissolved in 20 ml. of benzene and chromatographed on a 20 cm. x 5 cm. alumina column. The pure 2-phenylamino-4,6-dichloropyrimidine is eluted with benzene/chloroform (volume ratio 1:1) as eluting agent. It has a melting point of 111- 112.

(b) Step (b) of Example 108 is then repeated, but using 48 g. of 2-phenylarnino-4,6-dichloro-pyrimidine as starting material, and, since the desired product does not precipitate, it is necessary to subject the reaction mixture to steam distillation. An orange-colored resin is obtained which is dissolved in four times its amount (about 120 ml.) of ethanol at 80. Upon cooling, 30 g. of purified 2 phenylamino 4 ethylamino 6 chloro-pyrimidine crystallizes. It is separated by filtration and dried, and has a melting point of l03l04.

(0) Step (0) of Example 108 is repeated with this intermediate and a brown-colored syrupy product consisting of 2-phenylamino-4-ethylamino-6-(ti-hydroxyethylamino) pyrimidine is obtained which can be used directly as coupling component in each of the preceding examples, in lieu of the coupling components used therein.

Example Step (at) of Example 108 is repeated, but in lieu of 93 g. of aniline, there are used 61 g. of Z-amino-ethanol;

21 from the resulting mixture of two isomers, the Z-(B-hydroxyethylamino3-4,6-dichloro-pyrimidine is ilsoated, and steps (b) and (c) of Example 109 are then repeated but using aniline in lieu of 2-amino-ethanol in step (c).

2 (,3 hydroxyethylamino) 4 phenylamino 6 ethylamino-pyrimidine is obtained which can be used as coupling component in the preceding Examples 1 to 104 in lieu of the coupling components used therein.

For instance, by repeating the procedure of Example 1, in which the diazonium compound from l-amino-2,4-dinitro-6-chloro-benzene is used as diazo component, and employing as coupling component therein the abovedescribed pyrimidine, there is obtained the dyestufI of the formula:

which dyes polyethyleneglycol terephthalate fibers in pure red shades of good all round fastness properties.

We claim:

1. A monoazo dyestutf of the formula:

wherein A represents:

(a) a phenyl radical substituted as follows:

(i) by a first substituent selected from nitro, cyano, fluorine, chlorine, bromine, trifluoromethyl, lower alkanoyl, benzoyl, lower alkylsulfonyl, phenylsulfonyl, lower alkylphenyl-sulfonyl, phenoxysulfonyl, lower alkylphenoxysulfonyl, lower-alkoxycarbonyl, hydroxy-lower alkovycarbonyl, or a substituent of the formula:

wherein Q represents SO or wherein R and R represents lower alkyl, R represents phenyl having substituents selected from hydrogen, lower alkyl, lower alkoxy, chlorine, bromine and cyano; one of R and R represents alkyl of from 2 to 5 carbon atoms substituted by the group OR which group represents hydroxy, lower alkoxy, lower alkoxy-lower alkoxy, hydroxy-lower alkoxy, cyclohexyloxy, phenyl-lower alkoxy, phenoxy, lower alkyl-phenoxy, alkanoyloxy of from 2 to 5 carbon atoms, benzoyloxy, lower alkoxycarbonyloxy, phenyl-sulfonyloxy or lower alkyl-phenylsulfonyloxy, and the other one of R and R represents the same as the first one defined, supra, or hydrogen, lower alkyl, cyclohexyl or phenyl-lower alkyl. 2. A monoazo dyestutf as claimed in claim 1, wherein: A represents a phenyl radical as defined under (a) one of the said first and second substituents of which is in oand the other in p-position to the adjoining azo bridge. 3. A monoazo dyestuff as defined in claim 1, wherein: A represents a benzothiazolyl radical as defined under (b). 4. A monoazo dyestutr as defined in claim 2, wherein A is of the formula:

wherein: Z represents hydrogen, nitro, cyano, chlorine or bromine, and Z has the foresaid meaning.

R represents phenyl having substituents selected from hydrogen, lower alkyl and lower alkoxy, one of R and R represents lower alkyl substituted by hydroxy, lower alkoxy or alkanoyloxy of from 2 to 5 carbon atoms, and the other R of the pair of R and R represents optionally substituted lower alkyl, any substituent of which is selected from lower alkoxy and alkanoyloxy of from 2 to 5 carbon atoms. 6. A monoazo dyestuif as defined in claim 3, wherein: R represents phenyl having substituents selected from hydrogen, lower alkyl and lower alkoxy, one of R and R represents lower alkyl substituted by hydroxy, lower alkoxy, or alkanoyloxy of from 2 to 5 carbon atoms, and the other R of the pair of R and R represents lower alkyl which is unsubstituted or substituted by lower alkoxy or alkanoyloxy of from 2 to 5 carbon atoms. 7. A monoazo dyestutf as defined in claim 5, wherein R represents hydrogen, methyl or methoxy.

8. A monoazo dyestuff as defined in claim 6, wherein R represents hydrogen, methyl or methoxy.

9. A dye consisting of a mixture of a first dyestufi of the formula:

and a second dyestuff of the formula:

Z3 NHR3 N Z1 NIT-R9 wherein:

of Z Z and Z one Z represents the nitro group, a

second Z represents hydrogen, the nitro, cyano, methylsulfphonyl or ethylsulphonyl group, chlorine or bromine, and the third Z represents hydrogen, chlorine or bromine,

R represents hydrogen, the methyl or methoxy group,

and,

one of R and R represents alkyl of from 2 to carbon atoms substituted by the group OR which group represents hydroxy, lower alkoxy or alkanoyloxy of from 2 to 5 carbon atoms.

and the other one of R and R represents lower alkyl, which is unsubstituted or substituted by alkanoyloxy of from 2 to 5 carbon atoms or lower alkoxy.

the weight ratio of said first to said second dyestutf ranging from about 10:1 to about 1:10. 10. A disazo dyestuff of the formula:

TIM

wherein:

R represents phenyl having substituents selected from hydrogen, lower alkyl, lower alkoxy, chlorine, bromine and cyano;

one of R and R represents alkyl of from 2 to 5 carbon atoms substituted by the group OR which group represents hydroxy, lower alkoxy, lower alkoxy-lower alkoxy, hydroxy-lower alkoxy, cyclohexyloxy, phenyllower alkoxy, phenoxy, lower alkyl-phenoxy, alkanoyloxy of from 2 to 5 carbon atoms, benzoyloxy, lower alkoxycarbonyloxy, phenyl-sulfonyloxy, or lower alkylphenyl-sulfonyloxy, and

the other one of R and R represents the same as the first one defined, supra, or hydrogen, alkyl of from 1 to 12 carbon atoms, cyclohexyl or phenyl-lower alkyl,

each of R and R represents hydrogen, lower alkyl, or

lower alkoxy,

m represents a number from 1 to 3,

n represents a number from 1 to 2.

11. A dyestufi? as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

12. A dyestuif as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

13. A dyestuff as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

H-CHzCHzOC OCH:

14. A dyestuff as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

15. A dyestuff as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

16. A dyestuff as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

17. A dyestuff as defined in claim 9, which consists of a mixture of the two isomers defined by the formula:

0 CH3 NH- CHARLES B. PARKER, Primary Examiner D. M. PAPUGA, Assistant Examiner US. Cl. X.R. 

